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Absorption, phase transfer processes

The process in which chemicals become associated with solid phases is generally referred to as sorption. It is absorption if the molecules attach to a two-dimensional surface, while it is absorption if the molecules penetrate into a three-dimensional matrix. This phase transfer process may involve vapor molecules or dissolved molecules associating with solid phases. [Pg.277]

Ordinary diffusion involves molecular mixing caused by the random motion of molecules. It is much more pronounced in gases and Hquids than in soHds. The effects of diffusion in fluids are also greatly affected by convection or turbulence. These phenomena are involved in mass-transfer processes, and therefore in separation processes (see Mass transfer Separation systems synthesis). In chemical engineering, the term diffusional unit operations normally refers to the separation processes in which mass is transferred from one phase to another, often across a fluid interface, and in which diffusion is considered to be the rate-controlling mechanism. Thus, the standard unit operations such as distillation (qv), drying (qv), and the sorption processes, as well as the less conventional separation processes, are usually classified under this heading (see Absorption Adsorption Adsorption, gas separation Adsorption, liquid separation). [Pg.75]

In processing, it is frequently necessary to separate a mixture into its components and, in a physical process, differences in a particular property are exploited as the basis for the separation process. Thus, fractional distillation depends on differences in volatility. gas absorption on differences in solubility of the gases in a selective absorbent and, similarly, liquid-liquid extraction is based on on the selectivity of an immiscible liquid solvent for one of the constituents. The rate at which the process takes place is dependent both on the driving force (concentration difference) and on the mass transfer resistance. In most of these applications, mass transfer takes place across a phase boundary where the concentrations on either side of the interface are related by the phase equilibrium relationship. Where a chemical reaction takes place during the course of the mass transfer process, the overall transfer rate depends on both the chemical kinetics of the reaction and on the mass transfer resistance, and it is important to understand the relative significance of these two factors in any practical application. [Pg.573]

A thorough discussion of the mechanisms of absorption is provided in Chapter 4. Water-soluble vitamins (B2, B12, and C) and other nutrients (e.g., monosaccharides, amino acids) are absorbed by specialized mechanisms. With the exception of a number of antimetabolites used in cancer chemotherapy, L-dopa, and certain antibiotics (e.g., aminopenicillins, aminoceph-alosporins), virtually all drugs are absorbed in humans by a passive diffusion mechanism. Passive diffusion indicates that the transfer of a compound from an aqueous phase through a membrane may be described by physicochemical laws and by the properties of the membrane. The membrane itself is passive in that it does not partake in the transfer process but acts as a simple barrier to diffusion. The driving force for diffusion across the membrane is the concentration gradient (more correctly, the activity gradient) of the compound across that membrane. This mechanism of... [Pg.43]

The chain fragments formed by the recombination of free radicals can be reconverted into radicals by a variety of reinitiation processes, some of which are listed in Table 1. Such reactions can occur in the gas phase via electron collision and on the polymer surface by impact of charged particles or photon absorption. Reinitiation may also be induced in both the gas phase and on the polymer surface by hydrogen transfer reactions. These last processes are similar to the chain transfer processes which occur during homogeneous polymerization. Expressions for the rates of reinitiation are given by Eqns. 20 through 23. [Pg.53]

Phosphorescence corresponds to a different relaxation process. After the absorption phase, corresponding to the transfer of one electron into the Si level (singlet state), a spin inversion can occur if vibrational relaxation is slow, leading the electron to a T, state (triplet state) that is slightly more stable. Flence, return to the ground electronic state will be slower because it involves another spin inversion for this electron. For this reason, radiative lifetimes for phosphorescence can be up to 108 times greater than for fluorescence. [Pg.223]

Diffusion through a stagnant film, as in absorption or stripping processes involving the transfer of a single component between liquid and vapor phases. Since there is a concentration gradient... [Pg.399]

In these types of laboratory reactor, the flow of the liquid is very carefully controlled so that, although the mass transfer step is coupled with the chemical reaction, the mass transfer characteristics can be disentangled from the reaction kinetics. For some reaction systems, absorption of the gas concerned may be studied as a purely physical mass transfer process in circumstances such that no reaction occurs. Thus, the rate of absorption of C02 in water, or in non-reactive electrolyte solutions, can be measured in the same laboratory contactor as that used when the absorption is accompanied by the reaction between C02 and OH ions from an NaOH solution. The experiments with purely physical absorption enable the diffusivity of the gas in the liquid phase DL to be calculated from the average rate of absorption per unit area of gas-liquid interface NA and the contact time te. As shown in Volume 1, Chapter 10, for the case where the incoming liquid contains none of the dissolved gas, the relationship is ... [Pg.224]

In contrast to continuous packed bed columns, each stage, whether cocurrent or countercurrent, can be considered to be at equilibrium for many multi-phase mass-transfer processes such as distillation, absorption, extraction etc. Such stages are usually called ideal stages . [Pg.339]

Definitions Gas absorption is a unit operation in which soluble components of a gas mixture are dissolved in a liquid. The inverse operation, called stripping or desorption, is employed when it is desired to transfer volatile components from a liquid mixture into a gas. Both absorption and stripping, in common with distillation (Sec. 13), make use oF special equipment for bringing gas and liquid phases into intimate contact. This section is concerned with the design of gas-liquid contacting equipment, as well as with the design of absorption and stripping processes. [Pg.6]

Adsorption, absorption, and sorption are terms used to describe the uptake of a solute by another phase. Adsorption describes the concentration of a solute at the interface of two phases, while absorption describes the process when a solute is transferred from the bulk state of one phase into the bulk state of the other phase (Hassett and Banwart, 1989). The term sorption is used frequently in environmental situations to denote the uptake of a solute by a solid (soil or sediment or component of soil) without reference to a specific mechanism, or when the mechanism is uncertain. [Pg.163]

Liquid-liquid extraction involves contacting the feed stream (raffinate stream) with an immiscible liquid solvent in which one or more of the feed stream components is soluble. The component or components that are absorbed by this solvent are called the solute. Thus two different liquid phases are formed after addition or mixing of the solvent with the feed. The component that is more soluble in the solvent than in the feed will transfer to the solvent, a process known as absorption. The transferred component or components is called the solute. [Pg.259]

Equilibrium calculations are useful in the design or operation of a flue gas desulfurization (FGD) facility and provide the necessary foundation for complex process simulation (e.g., absorber modeling) (3). Since S02 absorption into FGD slurries is a mass transfer process which is primarily limited by liquid phase resistance for most commercial applications, the solution composition, in terms of alkaline species, is very critical to the performance of the system. Accurate prediction of solution composition via equilibrium models is essential to establishing driving forces for mass transfer, and ultimately in predicting system performance. [Pg.228]

Besides fluid mechanics, thermal processes also include mass transfer processes (e.g. absorption or desorption of a gas in a liquid, extraction between two liquid phases, dissolution of solids in liquids) and/or heat transfer processes (energy uptake, cooling, heating, drying). In the case of thermal separation processes, such as distillation, rectification, extraction, and so on, mass transfer between the respective phases is subject to thermodynamic laws (phase equilibria) which are obviously not scale dependent. Therefore, one should not be surprised if there are no scale-up rules for the pure rectification process, unless the hydrodynamics of the mass transfer in plate and packed columns are under consideration. If a separation operation (e.g. drying of hygroscopic materials, electrophoresis, etc.) involves simultaneous mass and heat transfer, both of which are scale-dependent, the scale-up is particularly difficult because these two processes obey different laws. [Pg.149]

Current multimedia models are inadequate in many respects. Description of intermedia transport across the soil-air and unsaturated soil-saturated soil zones suffers from the absence of a suitable theory for multiphase transport through the multiphase soil matrix. These phenomena are crucial in describing pollutant migration associated with hazardous chemical waste sites. Existing unsaturated-zone soil transport models fail to include mass transfer limitations associated with adsorption and desorption and with absorption and volatilization processes. Rather, most models assume equilibrium among the soil-air, soil-solid, solid-water, and soil-contaminant phases. [Pg.273]

Killion and Garimella conducted comprehensive critical reviews of analytical and numerical models [44] and experimental investigations [45] of absorption heat and mass transfer. Killion and Garimella [44] found that most of the literature on absorption heat and mass transfer work has focused on the particularly simplified case of absorption in laminar vertical films of LiBr/HjO. Fewer researchers have considered the important situations of wavy films, turbulent films, and films on horizontal tubes. They pointed out that attention must be paid to droplets and waves on horizontal tubes, and to the potential interaction of the heat and mass transfer process on the film hydrodynamics, surface wetting, and heat transfer in the vapor phase. In their review of experimental... [Pg.350]


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See also in sourсe #XX -- [ Pg.158 ]




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